Mb 12 recalls
The FDA has published 1 recall involving Mb 12 since 2016. The latest was reported on 15 Jun 2016. Most were for sterility. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 15 Jun 2016
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why mb 12 is recalled
Companies
By year
All mb 12 recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | MB 12/HXB 12/FA/P5P/(LIDO 0.1 %), 2MG/2MCi/20MG/6.5MG/ML recalled | Well Care Compounding Pharmacy | Sterility | NV |
Should you stop taking Mb 12?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.